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Support for SMEs in, or looking to enter, the medical technologies market.
Guiding principles for the use of Predetermined Change Control Plans (PCCPs) for managing rapid product changes.
Service providers or government departments installing networking technologies in government shared buildings, known as hub buildings.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How schools can enrol iPads in Apple School Manager (ASM), set up iPads and make the most out of them.
How schools should setup a Microsoft Windows laptop or tablet before lending the device to a child, family or young person.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
The Medicines and Healthcare products Regulatory Agency (MHRA), US Food and Drug Administration (FDA) and Health Canada have collaborated to identify five guiding principles for the development of predetermined change control plans (PCCPs). These guiding principles for PCCPs aim to...
Order a certificate of free sale to export medical devices outside the UK.
Information about the EU Regulations and their implementation in Northern Ireland
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